I hope you still check this site out. Can you give me some tips on how to live with HS2 in mouth? I am very depressed to have it in my lip than lower part. You know how it is. I just don't know how much longer I can take this suffering. I can't let people know what illness I am having, lied about what illness I have, can attend a lot of social gatherings if there is outbreak in lip. I want to die.